Tetraethylene Glycol → 1-Phenyl-2,5,8,11,14,17,20,23-octaoxapentacosan-25-ol
Reaction equation
[H-].[Na+].[CH2:3]([OH:15])[CH2:4][O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13]O.S([O-])(=O)(=O)C.[CH2:21]([O:28][CH2:29][CH2:30][O:31][CH2:32][CH2:33][O:34][CH2:35][CH2:36][O:37][CH2:38][CH2:39][OH:40])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>O1CCCC1>[CH2:21]([O:28][CH2:29][CH2:30][O:31][CH2:32][CH2:33][O:34][CH2:35][CH2:36][O:37][CH2:38][CH2:39][O:40][CH2:13][CH2:12][O:11][CH2:10][CH2:9][O:8][CH2:7][CH2:6][O:5][CH2:4][CH2:3][OH:15])[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1Participants
Procedure
To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of monodispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of monodispersed tetraethylene glycol monobenzylether 24 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the monodispersed compound 25 as a clear oil (2.62 g, 34% yield).
Workup
- additionwas added dropwise
- stirringthe reaction mixture was stirred overnight
- customThe crude reaction mixture
- filtrationwas filtered through Celite (washed, CH2Cl2, 250 mL)
- washthe filtrate was washed H2O, dried MgSO4
- customevaporated to dryness
- customThe resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1)
- customchromatographed (silica, chloroform/methanol, 25:1)
Sources & evidence
- ORD record
- ord-c7fe8d4a2b25441ab25a6b914e431c6a
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166571B2
Reaction notes
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